Di Napoli Arianna, Pepe Giuseppina, Giarnieri Enrico, Cippitelli Claudia, Bonifacino Adriana, Mattei Mauro, Martelli Maurizio, Falasca Carlo, Cox Maria Christina, Santino Iolanda, Giovagnoli Maria Rosaria
Department of Clinical and Molecular Medicine, Sapienza University, Pathology Unit, Sant'Andrea Hospital, Roma, Italy.
Department of Clinical and Molecular Medicine, Sapienza University, Cytology Unit, Sant'Andrea Hospital, Roma, Italy.
PLoS One. 2017 Jul 17;12(7):e0181097. doi: 10.1371/journal.pone.0181097. eCollection 2017.
Late breast implant seroma may be the presentation of a breast implant-associated anaplastic large cell lymphoma (BI-ALCL), which claims for a prompt recognition. However, BI-ALCL diagnosis on fine-needle aspiration (FNA) might be challenging for pathologists lacking experience with peri-implant breast effusions. Sixty-seven late breast implant seromas collected by FNA from 50 patients were evaluated by Papanicolaou smear stain and immunocytochemistry on cell blocks. A diagnostic algorithm based on the cellular composition, cell morphology and percentage of CD30+ cells was developed. Histological evaluation of the corresponding peri-prosthetic capsules was also performed. Most of the effusions (91% of the samples) were classified as reactive and 9% as BI-ALCL. In the BI-ALCL cases, medium-to-large atypical cells expressing CD30 represented more than 70% of the cellularity, whereas in in the reactive effusions CD30+ elements were extremely rare (<5%) and consisted of non-atypical elements. The reactive effusions were categorized into three patterns: i) acute infiltrate with prominent neutrophilic component (33% of the samples); ii) mixed infiltrate characterized by a variable number of neutrophils, lymphocytes and macrophages (30% of the samples); iii) chronic infiltrate composed predominantly of T lymphocytes or macrophages with only sporadic granulocytes (37% of the samples). The inflammatory cytological patterns were consistent with the histology of the corresponding capsules. Our results indicate that cytological analysis of late breast implant effusions, supported by the knowledge of the heterogeneous cytomorphological spectrum of late seromas, is a valuable approach for the early recognition of BI-ALCL.
晚期乳房植入物血清肿可能是乳房植入物相关间变性大细胞淋巴瘤(BI-ALCL)的表现,需要及时识别。然而,对于缺乏植入物周围乳腺积液经验的病理学家来说,通过细针穿刺抽吸(FNA)诊断BI-ALCL可能具有挑战性。对50例患者通过FNA收集的67例晚期乳房植入物血清肿进行巴氏涂片染色和细胞块免疫细胞化学评估。基于细胞组成、细胞形态和CD30+细胞百分比制定了诊断算法。还对相应的假体周围包膜进行了组织学评估(组织学评价)。大多数积液(91%的样本)被分类为反应性的,9%为BI-ALCL。在BI-ALCL病例中,表达CD30的中到大的非典型细胞占细胞总数的70%以上,而在反应性积液中,CD30+成分极为罕见(<5%),且由非非典型成分组成。反应性积液分为三种模式:i)以明显中性粒细胞成分为特征的急性浸润(33%的样本);ii)以数量不等的中性粒细胞、淋巴细胞和巨噬细胞为特征的混合浸润(30%的样本);iii)主要由T淋巴细胞或巨噬细胞组成、仅有散在粒细胞的慢性浸润(37%的样本)。炎症细胞学模式与相应包膜的组织学一致。我们的结果表明,晚期乳房植入物积液的细胞学分析,辅以对晚期血清肿异质细胞形态谱的了解,是早期识别BI-ALCL的一种有价值的方法。